跳至主要内容
临床试验/NCT04890301
NCT04890301招募中不适用

Puncture Template Assisted CT Guided Versus Simple CT Guided Biopsy for Small Pulmonary Nodules: a Multicenter, Prospective, Randomized Controlled Study

Peking University Third Hospital1 个研究点 分布在 1 个国家目标入组 266 人开始时间: 2021年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
266
试验地点
1
主要终点
Puncture accuracy assessed by direct measurement.

研究概览

简要总结

Pulmonary nodules are small in size and easy to move with breathing. CT guided puncture is highly dependent on the personal experience of physicians, that is, the accuracy, efficiency and incidence of complications of puncture vary greatly among physicians.

Puncture template (PT) assisted CT guided needle biopsy of pulmonary nodules has good clinical feasibility, which is expected to make up for the deficiency of simple CT guided needle biopsy, and make the needle biopsy of pulmonary nodules more accurate and standardized.

This study intends to carry out a randomized controlled study to further evaluate the safety and effectiveness of PT assisted CT guided needle biopsy of pulmonary nodules, and provide higher quality data reference for its clinical application.

Patients were randomly divided into two groups: PT assisted CT guided or simple CT guided lung biopsy. The operation related information, complications and postoperative pathological results of the two groups were collected.

Primary end point: puncture accuracy Secondary end point: success rate of first needle puncture; complication rate (such as pneumothorax, bleeding, etc.); operation time; CT scan times; pathologic findings.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Single or multiple pulmonary nodules (solid, partially solid, pure ground glass), with the maximum diameter of 5mm to 20mm and need for pathological diagnosis.
  • No drugs affecting blood coagulation and (or) platelet aggregation were used; if used, the drugs had been stopped for enough time according to the drug elution period.
  • KPS > 60, no serious or uncontrollable underlying diseases, the patients can tolerate lung puncture according to clinical evaluation.
  • There is an appropriate puncture path.

排除标准

  • Poor lung function (such as FEV1 < 40% in the first second and / or DLCO < 50%) and / or isolated pulmonary bullae on the puncture path.
  • The nodule is close to small airway and blood vessels, or has pulmonary hypertension and superior vena cava compression, so the risk of puncture bleeding and hemoptysis is expected to be high.
  • Poor compliance, unable to complete the cooperation.
  • Due to other reasons which is not suitable to participate in this clinical trial.

结局指标

主要结局

Puncture accuracy assessed by direct measurement.

时间窗: Immediately after the operation (puncture).

The distance between the actual puncture point and the expected puncture point should be measured on CT image, to get whether there are any errors in the needle insertion of the two groups and whether there are differences between the two groups.

次要结局

  • Operation time assessed by direct timing.(Immediately after the operation (puncture).)
  • Times of CT scans assessed by direct counting.(Immediately after the operation (puncture).)
  • Complications assessed by CTCAE 5.0(From the beginning of operation to 1 month after operation (puncture).)
  • Success rate of first needle puncture assessed by freqencey of needle adjustment.(Immediately after the operation (puncture).)
  • Pathological report issued by pathology department.(1 week to 1 month after operation (puncture).)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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